Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.10 (A)
Location

Chromosome X:135983290 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60088348

HGVS name

X:g.135983290G>A

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 4 transcripts and has 4027 sample genotypes.

Variant displays